ion exchange high performance liquid chromatography Search Results


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International Federation of Clinical Chemistry and Laboratory Medicine ion-exchange high-performance liquid chromatography
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Wnt-1 <t>siRNA</t> induces apoptosis. (A) Annexin V analysis of apoptosis induced by Wnt-1 siRNA. From top to bottom: MCF-7 cancer cells were treated without siRNA (vehicle only), 100 nM nonsilencing control siRNA, and 100 nM Wnt-1 siRNA, respectively. FL1-H represents Annexin V-FITC staining and FL3-H represents PI staining. (B) Western blot analysis after Wnt-1 siRNA treatments (100 nM for 72 hours); nonsilencing siRNA served as control. MCF-7 cells were treated with either Wnt-1 siRNA or nonsilencing siRNA control. β-Actin served as loading control.
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Biochrom ion-exchange liquid chromatography for hydrolyzed samples
Wnt-1 <t>siRNA</t> induces apoptosis. (A) Annexin V analysis of apoptosis induced by Wnt-1 siRNA. From top to bottom: MCF-7 cancer cells were treated without siRNA (vehicle only), 100 nM nonsilencing control siRNA, and 100 nM Wnt-1 siRNA, respectively. FL1-H represents Annexin V-FITC staining and FL3-H represents PI staining. (B) Western blot analysis after Wnt-1 siRNA treatments (100 nM for 72 hours); nonsilencing siRNA served as control. MCF-7 cells were treated with either Wnt-1 siRNA or nonsilencing siRNA control. β-Actin served as loading control.
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Wnt-1 <t>siRNA</t> induces apoptosis. (A) Annexin V analysis of apoptosis induced by Wnt-1 siRNA. From top to bottom: MCF-7 cancer cells were treated without siRNA (vehicle only), 100 nM nonsilencing control siRNA, and 100 nM Wnt-1 siRNA, respectively. FL1-H represents Annexin V-FITC staining and FL3-H represents PI staining. (B) Western blot analysis after Wnt-1 siRNA treatments (100 nM for 72 hours); nonsilencing siRNA served as control. MCF-7 cells were treated with either Wnt-1 siRNA or nonsilencing siRNA control. β-Actin served as loading control.
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Biomol GmbH high-performance liquid chromatography coupled with tandem mass spectrometry in a linear ion trap
Wnt-1 <t>siRNA</t> induces apoptosis. (A) Annexin V analysis of apoptosis induced by Wnt-1 siRNA. From top to bottom: MCF-7 cancer cells were treated without siRNA (vehicle only), 100 nM nonsilencing control siRNA, and 100 nM Wnt-1 siRNA, respectively. FL1-H represents Annexin V-FITC staining and FL3-H represents PI staining. (B) Western blot analysis after Wnt-1 siRNA treatments (100 nM for 72 hours); nonsilencing siRNA served as control. MCF-7 cells were treated with either Wnt-1 siRNA or nonsilencing siRNA control. β-Actin served as loading control.
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ARKRAY Inc ion-exchange high-performance liquid chromatography
Wnt-1 <t>siRNA</t> induces apoptosis. (A) Annexin V analysis of apoptosis induced by Wnt-1 siRNA. From top to bottom: MCF-7 cancer cells were treated without siRNA (vehicle only), 100 nM nonsilencing control siRNA, and 100 nM Wnt-1 siRNA, respectively. FL1-H represents Annexin V-FITC staining and FL3-H represents PI staining. (B) Western blot analysis after Wnt-1 siRNA treatments (100 nM for 72 hours); nonsilencing siRNA served as control. MCF-7 cells were treated with either Wnt-1 siRNA or nonsilencing siRNA control. β-Actin served as loading control.
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ARKRAY Inc ion-exchange high performance liquid chromatography arkray adams a1c automated platform
Wnt-1 <t>siRNA</t> induces apoptosis. (A) Annexin V analysis of apoptosis induced by Wnt-1 siRNA. From top to bottom: MCF-7 cancer cells were treated without siRNA (vehicle only), 100 nM nonsilencing control siRNA, and 100 nM Wnt-1 siRNA, respectively. FL1-H represents Annexin V-FITC staining and FL3-H represents PI staining. (B) Western blot analysis after Wnt-1 siRNA treatments (100 nM for 72 hours); nonsilencing siRNA served as control. MCF-7 cells were treated with either Wnt-1 siRNA or nonsilencing siRNA control. β-Actin served as loading control.
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PerSeptive Biosystems Inc ion-exclusion high-performance liquid chromatography poroshq column
Wnt-1 <t>siRNA</t> induces apoptosis. (A) Annexin V analysis of apoptosis induced by Wnt-1 siRNA. From top to bottom: MCF-7 cancer cells were treated without siRNA (vehicle only), 100 nM nonsilencing control siRNA, and 100 nM Wnt-1 siRNA, respectively. FL1-H represents Annexin V-FITC staining and FL3-H represents PI staining. (B) Western blot analysis after Wnt-1 siRNA treatments (100 nM for 72 hours); nonsilencing siRNA served as control. MCF-7 cells were treated with either Wnt-1 siRNA or nonsilencing siRNA control. β-Actin served as loading control.
Ion Exclusion High Performance Liquid Chromatography Poroshq Column, supplied by PerSeptive Biosystems Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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A Menarini Diagnostics S r l ion exchange high performance liquid chromatography
Wnt-1 <t>siRNA</t> induces apoptosis. (A) Annexin V analysis of apoptosis induced by Wnt-1 siRNA. From top to bottom: MCF-7 cancer cells were treated without siRNA (vehicle only), 100 nM nonsilencing control siRNA, and 100 nM Wnt-1 siRNA, respectively. FL1-H represents Annexin V-FITC staining and FL3-H represents PI staining. (B) Western blot analysis after Wnt-1 siRNA treatments (100 nM for 72 hours); nonsilencing siRNA served as control. MCF-7 cells were treated with either Wnt-1 siRNA or nonsilencing siRNA control. β-Actin served as loading control.
Ion Exchange High Performance Liquid Chromatography, supplied by A Menarini Diagnostics S r l, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
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Image Search Results


Wnt-1 siRNA induces apoptosis. (A) Annexin V analysis of apoptosis induced by Wnt-1 siRNA. From top to bottom: MCF-7 cancer cells were treated without siRNA (vehicle only), 100 nM nonsilencing control siRNA, and 100 nM Wnt-1 siRNA, respectively. FL1-H represents Annexin V-FITC staining and FL3-H represents PI staining. (B) Western blot analysis after Wnt-1 siRNA treatments (100 nM for 72 hours); nonsilencing siRNA served as control. MCF-7 cells were treated with either Wnt-1 siRNA or nonsilencing siRNA control. β-Actin served as loading control.

Journal:

Article Title: A Monoclonal Antibody against Wnt-1 Induces Apoptosis in Human Cancer Cells 1

doi:

Figure Lengend Snippet: Wnt-1 siRNA induces apoptosis. (A) Annexin V analysis of apoptosis induced by Wnt-1 siRNA. From top to bottom: MCF-7 cancer cells were treated without siRNA (vehicle only), 100 nM nonsilencing control siRNA, and 100 nM Wnt-1 siRNA, respectively. FL1-H represents Annexin V-FITC staining and FL3-H represents PI staining. (B) Western blot analysis after Wnt-1 siRNA treatments (100 nM for 72 hours); nonsilencing siRNA served as control. MCF-7 cells were treated with either Wnt-1 siRNA or nonsilencing siRNA control. β-Actin served as loading control.

Article Snippet: The ion exchange high-performance liquid chromatography-purified siRNA (Wnt-1 siRNA and nonsilencing siRNA control, >97% pure) were purchased from Qiagen-Xeragon (Germantown, MD).

Techniques: Control, Staining, Western Blot